Diagnostic Technology, Inc.
FDA 510(k) medical device clearances.
Top product codes for Diagnostic Technology, Inc.
Recent clearances by Diagnostic Technology, Inc.
- K896378 — LYME-CHECK(TM) TEST KIT
- K903612 — EBV/EA-CHECK TM TEST KIT
- K890639 — RESUBMITTED EBV/IGM-CHECK TEST KIT
- K890819 — HSV-CHECK(TM) TEST KIT
- K891542 — EBNA-CHECK(TM) TEST KIT
- K871373 — EBV-CHECK(TM) TEST KIT (IGG)
- K864128 — CHLAMYDIA-CHECK(TM) DIRECT & CULTURE CONFIR. KIT
- K863408 — EBV/VCA-CHECK(TM) ANTIGEN SLIDES
- K860586 — PHA-2 CONVERSION PROGRAM FOR PLATELET ANALYSIS
- K860166 — PICOSCALE BLOOD CELL COUNTER, MODEL PS-5
- K853036 — PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1
- K841809 — COUNT-A-PART PLUS
- K842140 — PICOSCAL BLOOD CELL COUNTER PS-4
- K834345 — IM-CHECK
- K834372 — PHA-1 PROGRAMMABLE HEMATOLOGY ANALYZ
- K834346 — BHCG-CHECK
- K831466 — HCG-CHECK
- K831468 — B HCG-CHECK
- K831464 — ASO-CHECK
- K831463 — ANA-CHECK
- K831465 — CRP-CHECK
- K831467 — RA-CHECK
- K827289 — DIGITAL RADIOGRAPHY SYSTEM
- K820037 — SICKLE-CHECK
- K811063 — LASER-CAL
- K791750 — COUNTER-CHECK PLUS
- K791772 — COUNTER-CHECK PLUS NORMAL, HIGH ABN.
- K790025 — COUNTER CHECK, H001, H002, H003
Data sourced from openFDA. This site is unofficial and independent of the FDA.